REFERENCES
- Ellis, R. W. B., Sheldon, W. and Capon, N. B.: Gargoylism. Quart J Med 5:119–139, 1936.
- Dorfman, A.: Heritable diseases of connective tissues: The Hurler syndrome. In John B. Stanbury (Editor): The Metabolic Basis of Inherited Disease. Ed. 2. New York, McGraw-Hill Book Company, 1966, chap. 41, pp. 963–994.
- Lorincz, A. E.: Hurler's syndrome. In C. H. Carter (Editor): Medical Aspects of Mental Retardation. Springfield, Illinois, Charles C Thomas, 1965, pp. 628–650.
- McKusick, V. A.: Heritable Disorders of Connective Tissue. Ed. 3. St. Louis, The C. V. Mosby Company, 1966.
- Krovetz, L. J., Lorincz, A. E. and Schiebler, J. L.: Cardiovascular manifestations of the Hurler syndrome. Circulation 31:132–141, 1965.
- Dorfman, A.: Studies on the biochemistry, of connective tissue. Pediatrics 22:576–588, 1958.
- Callahan, W. P. and Lorincz, A. E.: Hepatic infrastructure in the Hurler syndrome. Amer J Path 48:277–298, 1966.
- Caffey, J.: Gargoylism (Hunter-Hurler disease, dysostosis multiplex, lipochondrodystrophy). Prenatal and neonatal bone lesions and their early postnatal evaluation. Amer J Roentgen 67:715–731, 1952.
- Horrigan, W. D. and Baker, D. H.: Gargoylism: A review of the roentgen skull changes with description of a new finding. Amer J Roentgen 86: 473–477, 1961.